Infections of the human colon are difficult to study mechanistically because of the absence of in vitro model systems that mimic the limited oxygen environment of the colon. In this project, we propose to use a human intestinal model system based on cylindrical silk scaffolds that serve as the backbone for human epithelial and sub-epithelial tissues. This proposed bioengineered 3D model system will be used to address the details of infection by the major human diarrheal pathogen, Clostridium difficile. Steps in C. difficile pathogenesis, such as spore germination, vegetative cell outgrowth, adherence, toxin production and epithelial cell damage will be studied in the tissue model.
In Aim 1, further development of the tissue model will be pursued. The tissue models will be incorporated into perfusion bioreactors capable of passing media of variable chemical compositions and low oxygen tension through the lumens at regulatable rates. The central, hollow core of the tissue model will thus mimic an intestinal lumen in which bacteria and host tissue will interact.
In Aim 2, a combination of single cell analysis using fluorescent reporter proteins and genetic analysis of mutants using TnSeq will be pursued to analyze the importance of bacterial factors for infection in the tissue model. The experiments proposed are designed to validate the bioengineered 3D intestinal model system as well as generate new information about the pathogenesis of C. difficile. Interaction between C. difficile and the human gut microbiota will be investigated in Aim 3. Microbiota will be established in the tissue model for these experiments.
Aim 4 will focus on testing the efficacy of several anti-infective strategies against C. difficile infection, using the scaffold tissue model. This project will establish the bioengineered intestine tissue model as a novel system for detailed, mechanistic analysis of infection by virtually all colonic pathogens, thereby providing the potential for major breakthroughs in the understanding of multiple aspects of intestinal infection.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program--Cooperative Agreements (U19)
Project #
1U19AI131126-01
Application #
9312412
Study Section
Special Emphasis Panel (ZAI1-BLG-M (J2))
Project Start
2017-04-07
Project End
2022-03-31
Budget Start
2017-03-01
Budget End
2018-02-28
Support Year
1
Fiscal Year
2017
Total Cost
$438,860
Indirect Cost
$135,687
Name
Tufts University
Department
Type
Domestic Higher Education
DUNS #
039318308
City
Boston
State
MA
Country
United States
Zip Code
02111
Zhou, Wenda; Chen, Ying; Roh, Terrence et al. (2018) Multifunctional Bioreactor System for Human Intestine Tissues. ACS Biomater Sci Eng 4:231-239
Shaban, Lamyaa; Chen, Ying; Fasciano, Alyssa C et al. (2018) A 3D intestinal tissue model supports Clostridioides difficile germination, colonization, toxin production and epithelial damage. Anaerobe 50:85-92
Chen, Ying; Zhou, Wenda; Roh, Terrence et al. (2017) In vitro enteroid-derived three-dimensional tissue model of human small intestinal epithelium with innate immune responses. PLoS One 12:e0187880